A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185052



Internal ID20752092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51170135..51174862hg38UCSC Ensembl
chr13:51744271..51748998hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384728
hg194728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495287
Supporting Variants
Samples
Known GenesLINC00371
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185052
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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